持续光照和慢性酒精中毒下wistar大鼠某些生化参数昼夜节律性的性别特征

D. Areshidze, M. A. Kozlova, L. Makartseva, Y. Kirillov
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引用次数: 0

摘要

背景:各级组织的生物系统都以功能过程的节奏为特征,这是生命物质的基本特性之一。哺乳动物复杂的昼夜节律是由遗传决定的,并受到内外环境周期性因素的可塑性调节。现代世界生物节律紊乱的重要因素包括光-暗交替的破坏,即所谓的光污染。酒精滥用仍然是现代社会最重要的医学和社会问题之一。酒精的一个重要影响是它对许多生理过程的昼夜节律的破坏性影响。目的:研究持续光照和慢性酒精中毒对Wistar大鼠生理生化指标昼夜动态的影响及其共同作用。材料与方法:选用200只和160只6月龄雌性近交系Wistar大鼠,体重350 - 15 g。大鼠分为8组。第一组(对照♂)保持固定光照状态(10点14分亮/暗,8点开灯,18点关灯)。第二组,雄性(n = 50)保持在与对照组相同的条件下,但以15%的乙醇随意水溶液代替水作为饮料,即慢性酒精中毒。第三组,雄性(n = 50)保持恒定光照。第四组,雄性(n = 50)也保持在恒定照明下,并随意饮用15%乙醇水溶液。第5组(对照组♀)雌性(n = 40),保持在固定的光照条件下(上午10:14亮/暗,8:00开灯,18:00关灯)。第六组,女性(n = 40)保持在与对照组相同的条件下,但接受15%的乙醇水溶液,而不是水作为饮料,即慢性酒精中毒。第7组,雌性(n = 40)保持恒定光照。第八组,雌性(n = 40)也保持在恒定光照下,并随意饮用15%乙醇水溶液。分别于9:00、15:00、21:00、3:00取血,测定AST、ALT、葡萄糖、总蛋白、白蛋白、总胆红素和直接胆红素的含量。使用余弦分析评估研究参数的昼夜节律性的可靠性。结果:证实慢性酒精中毒、持续光照及这些因素的共同作用导致两性大鼠的生化参数变化相似,但雌性大鼠的AST、总胆红素和直接胆红素水平在醉酒3周后发生变化,而雄性大鼠未观察到这种变化。反过来,慢性酒精中毒和黑暗剥夺的个体和联合效应导致大鼠的节律稳定发生显著变化,然而,总蛋白的昼夜节律以及两种类型的胆红素,在雌性中比在雄性中更能抵抗黑暗剥夺。结论:本研究证明,与雄性相比,三周的慢性酒精中毒会导致雌性大鼠的生化特征发生更显著的变化。与此同时,所研究的雌性生物生化参数的昼夜节律比雄性更能抵抗黑暗剥夺,只有在慢性酒精中毒和持续光照的共同作用下才会被破坏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex features of the circadian rhythmicity of some biochemical parameters in wistar rats under constant lighting and chronic alcohol intoxication
BACKGROUND: Biological systems of all levels of organization are characterized by the rhythm of functioning processes, which are one of the fundamental properties of living matter. The complex of circadian rhythms of mammals, being genetically determined, is quite plastically modulated by the action of periodic factors of the external and internal environment. Significant factors in the disorganization of biorhythms in the modern world include a violation of the light-dark regime, so-called light pollution. Alcohol abuse remains one of the most important medical and social problems of modern society. One of the important effects of alcohol is its destructive effect on the circadian rhythms of many physiological processes. AIM: The aim of the research was to study the influence of constant lighting, chronic alcohol intoxication and joint effect of these factors on the diurnal dynamics of several biochemical parameters in Wistar rats of both sexes. MATERIALS AND METHODS: The study was conducted on 200 and 160 female outbred Wistar rats at the age of 6 months, weighing 350 15 g. Rats were divided into 8 groups. 1st group (control ♂) is kept at fixed light regime (light/dark 10:14 hours with lights on at 8:00 and off at 18:00). 2nd group, males (n = 50) is kept under the same conditions as the control, but receives a 15 % aqueous solution of ethanol ad libitum as a drink instead of water, i.e. is subjected to chronic alcohol intoxication. Group 3, males (n = 50) are kept under constant light. The 4th group, males (n = 50) are also kept under constant illumination and receive 15 % aqueous ethanol solution ad libitum as a drink. Group 5 (control ♀) females (n = 40), are kept at a fixed light regime (light/dark 10:14 am with lights on at 8:00 and off at 18:00). The 6th group, females (n = 40) are kept under the same conditions as the control, but receive 15 % aqueous ethanol solution ad libitum instead of water as a drink, i.e. subjected to chronic alcohol intoxication. Group 7, females (n = 40) are kept under constant light. The 8th group, females (n = 40) are also kept under constant light and receive 15 % aqueous ethanol solution ad libitum as a drink. In the blood samples taken at 9:00, 15:00, 21:00 and 3:00 hours the content of AST, ALT, glucose, total protein, albumin, total and direct bilirubin was measured. The reliability of circadian rhythmicity of studied parameters was assessed with use of cosinor analysis. RESULTS: It is established that the chronic alcohol intoxication, constant illumination and joint action of this factors lead to similar changes in biochemical parameters in rats of both sexes, but in female rats the level of AST, total and direct bilirubin changes as a result of three weeks of intoxication, which is not observed in males. In turn, both individual and joint effects of chronic alcohol intoxication and dark deprivation lead to significant changes in rhythmostasis in rats, however, circadian rhythms of total protein, as well as both types of bilirubin, are more resistant to dark deprivation in females than in males. CONCLUSIONS: The conducted study testifies that a three-week chronic alcohol intoxication causes more significant changes in the biochemical profile in female rats compared to males. At the same time, the studied circadian rhythms of the biochemical parameters of the organism of females turn out to be more resistant to dark deprivation than those of males, being destroyed only under the combined action of chronic alcohol intoxication and constant illumination.
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